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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485074Generated: October 30, 2026

2-(N-Benzyl-N-methylamino)ethyl 3-amino-2-butenoate → HCID 13363671, compound

https://huagongshe.com/reaction/485074

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(N-Benzyl-N-methylamino)ethyl 3-amino-2-butenoateHCID 12529188—
ReactantDimethyl 1-(3-nitrobenzylidene)-acetonylphosphonateHCID 53986679—
SolventIsopropanolHCID 3776—
ProductHCID 13363671HCID 1336367121.1%

Reaction Steps

To a mixture of 3.42 grams of dimethyl 1-(3-nitrobenzylidene)-acetonylphosphonate and 3.13 grams of 2-(N-benzyl-N-methylamino)-ethyl 3-aminocrotonate was added 50 ml of isopropanol and the mixture was heated to reflux for four hours with stirring. The reaction mixture was concentrated in vacuo, the residue was dissolved in ethyl acetate, to this was added 5% hydrochloric acid solution followed by separation, chloroform was added the lower layer followed by separation, the chloroform layer was washed with 5% calcium carbonate solution and then with water, and dried. Chloroform was evaporated in vacuo, the residue was purified by subjecting to silica gel column chromatography (100 grams of silica gel being used; eluting solution is ethyl acetate), and the resulting crystals were recrystallized from a mixture of ethyl acetate and ether to give 1.28 grams (yield 20%) of 2-(N-benzyl-N-methylamino)-ethyl 5-dimethoxyphosphinyl-2,6-dimethyl-4-(3-nitrophenyl)-1,4-dihydropyridine-3-carboxylate, pale yellow crystals, melting point 101°-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04535073
Source datasetuspto-grants-1985_08
ORD IDord-0f091b6f44bc495c9a5439d000075e70
Source noteuspto-grants-1985_08